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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Puberty, Precocious (D011629)
..Starting node ..Sexual precocity (C538542)
Child Nodes:
Sister Nodes:
..Adrenal Hypoplasia, Congenital, with Precocious Puberty (C564568)
..Familial Testotoxicosis (C536961)
..Hypotonia, Seizures, And Precocious Puberty (C567566)
..Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty (C567168)
..Precocious Puberty, Central (C562787)
..Sexual precocity (C538542)
..Spastic paraplegia with precocious puberty (C536874)
..Spondylodysplasia And Premature Pubarche (C567552)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10171
Name:	Sexual precocity
Definition:
Alternative IDs:
ParentIDs:	MESH:D011629
TreeNumbers:	C19.391.693/C538542
Synonyms:	Familial precocious puberty \|Idiopathic sexual precocity
Slim Mappings:	Endocrine system disease
Reference:	MedGen: C538542 MeSH: C538542 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants